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rs794728633

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728633(A;A)
Make rs794728633(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804443
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728633
ebirs794728633
HLIrs794728633
Exacrs794728633
Varsomers794728633
Maprs794728633
PheGenIrs794728633
hapmaprs794728633
1000 genomesrs794728633
hgdprs794728633
ensemblrs794728633
gopubmedrs794728633
geneviewrs794728633
scholarrs794728633
googlers794728633
pharmgkbrs794728633
gwascentralrs794728633
openSNPrs794728633
23andMers794728633
23andMe allrs794728633
SNP Nexus

SNPshotrs794728633
SNPdbers794728633
MSV3drs794728633
GWAS Ctlgrs794728633
Max Magnitude0
ClinVar
Risk rs794728633(A;A)
Alt rs794728633(A;A)
Reference rs794728633(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64571915A>T
CLNSRC
CLNACC RCV000182427.1,